Clinical genetics and dysmorphology: A unique pioneering experiences - Al-Mosawi, Aamir
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We have previously described our extensive experiences with clinical genetic and dysmorphology in a plethora of publications. In a previous study, we reported 43 children with uncommon, rare and very rare genetic and hereditary disorders whom were observed during three-year period (2016-2018). In that series , very rare genetic, the case number 104 of Sanjad-Sakati-Richardson-Kirk syndrome in the world, the case number 130 of Townes Brocks syndrome, and the case number 170 of Coffin Siris syndrome in the world. The aim of this paper is to describe our 2019 extraordinary new experiences with genetic disorders and dysmorphic syndromes.…mehr

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Produktbeschreibung
We have previously described our extensive experiences with clinical genetic and dysmorphology in a plethora of publications. In a previous study, we reported 43 children with uncommon, rare and very rare genetic and hereditary disorders whom were observed during three-year period (2016-2018). In that series , very rare genetic, the case number 104 of Sanjad-Sakati-Richardson-Kirk syndrome in the world, the case number 130 of Townes Brocks syndrome, and the case number 170 of Coffin Siris syndrome in the world. The aim of this paper is to describe our 2019 extraordinary new experiences with genetic disorders and dysmorphic syndromes.
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Autorenporträt
Aamir Jalal Al-Mosawi è medico consulente presso il Centro nazionale di formazione e sviluppo del Ministero della Salute iracheno e la Città medica di Baghdad. È stato capo della sede irachena del gruppo internazionale di scienziati Copernicus (2006-ottobre 2020). È anche membro del consiglio consultivo dell'Associazione internazionale dei collegi medici (IAMC), dal 2008.